Primary Device ID | 05060502570000 |
NIH Device Record Key | c859975b-ac0a-4b3a-94e6-94be432486b0 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Paryvara |
Version Model Number | TH-1412 |
Company DUNS | 221119216 |
Company Name | BOOT REMEDY LTD |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | false |
Lot Batch | false |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | false |
OTC Over-The-Counter | false |